Find Clarity for Your Family’s Genetic Health Journey
When you’re concerned about developmental challenges or suspect a genetic condition might be affecting your loved ones, the uncertainty can be overwhelming. Our SMC1A Gene Cornelia de Lange Syndrome Type 2 test provides the definitive answers you need to move forward with confidence and create the best possible care plan for your family.
Understanding the SMC1A Gene Test
This advanced genetic test specifically examines the SMC1A gene using Next-Generation Sequencing (NGS) technology – the gold standard in genetic diagnostics. The test identifies mutations that cause Cornelia de Lange Syndrome type 2, a condition that affects physical development, intellectual growth, and overall health. Unlike basic genetic screenings, our NGS approach provides comprehensive analysis with exceptional accuracy, giving you reliable results you can trust for making informed healthcare decisions.
Who Should Consider This Genetic Test?
This test is particularly important if you or your child experience:
- Unexplained developmental delays in early childhood
- Distinctive facial features including arched eyebrows and long eyelashes
- Growth restrictions or failure to thrive
- Intellectual disability or learning challenges
- Family history of genetic disorders or developmental conditions
- Multiple congenital abnormalities affecting limbs or organs
Early testing can provide crucial insights that help guide appropriate interventions and support services.
Why Early Detection Matters for Your Family’s Health
Getting tested isn’t just about diagnosis – it’s about empowerment. Understanding your genetic profile enables:
- Personalised Care Planning: Tailor medical interventions and therapies to specific needs
- Family Planning Guidance: Make informed decisions about future pregnancies
- Early Intervention Opportunities: Access support services when they’re most effective
- Reduced Diagnostic Uncertainty: End the cycle of unanswered questions and multiple specialist visits
- Peace of Mind: Replace anxiety with actionable information and clear next steps
Understanding Your Test Results
We know waiting for genetic test results can be stressful. That’s why we provide:
- Clear, Comprehensive Reports: Easy-to-understand results with detailed explanations
- Professional Genetic Counselling: Expert guidance to help interpret your results
- Family Pedigree Analysis: Understanding how genetic factors may affect other family members
- Actionable Recommendations: Specific next steps based on your unique results
- Ongoing Support: Access to resources and specialists who understand your situation
Your results will be ready within 3-4 weeks, and we’ll guide you through every step of understanding what they mean for your family.
Transparent Pricing – Exceptional Value
| Service | Regular Price | Special Price | Savings |
|---|---|---|---|
| SMC1A Gene Cornelia de Lange Syndrome Type 2 NGS Test | ZAR 6,700 | ZAR 2,650 | |
| Includes genetic counselling, comprehensive analysis, and detailed results interpretation | |||
Consider this investment in your family’s health: early diagnosis can prevent years of uncertainty and potentially save thousands in unnecessary medical consultations and tests.
Why South African Families Trust Oracle Genomics
- Nationwide Coverage: Accessible testing centres in Johannesburg, Cape Town, Durban, and Pretoria
- Medical Expertise: Partnered with leading dermatologists and genetic specialists
- Advanced Technology: State-of-the-art NGS testing for maximum accuracy
- Multiple Sample Options: Blood, extracted DNA, or simple blood spot on FTA card
- South African Focus: Understanding local healthcare needs and family dynamics
- Proven Track Record: Thousands of successful genetic tests conducted nationwide
Take the First Step Toward Genetic Clarity Today
Don’t let uncertainty dictate your family’s health journey. With our special pricing of ZAR 6,700, there’s never been a better time to get the answers you deserve.
Limited Time Offer: This special pricing of ZAR 6,700 won’t last forever. Secure your family’s genetic health today and take control of your healthcare journey.
Ready within 3-4 weeks | Nationwide coverage | Professional genetic counselling included
